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The Cost Accountant is responsible for manging cost accounting and fixed asset activities for Dendreon.
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The Regional Sales Manager is responsible for executing strategic sales plans and manages the Immunotherapy Sales Specialists to meet or exceed sales goals and customer satisfaction. This position leads a high performing sales team and manages all account activity within their designated region. This position continually develops the skills of individuals within his/her team to produce sales volume at or above the assigned region sales quota. This position reports to the National Director of Sales.
Extensive travel will be required. This job description has been designated to indicate the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required for company business needs from time to time. Preferred candidate locale is the state of California, however the following is acceptable: Denver, Phoenix, Seattle, and Las Vegas.
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Dendreon’s Immunotherapy Sales Specialist is responsible for achieving sales objectives in an assigned territory through the development, maintenance, and enhancement of the business. Customers include oncologists, urologists, nurses, pharmacists, pharmacy and therapeutics groups, tumor boards, teaching institutions, hospitals and formulary committees. The role is responsible for ensuring customer’s clinical conviction in the product as well as guiding the customer through the logistics process and seeing the sale through to its conclusion. The territory alignment is the capital in it's entirety.
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The Director/Sr Director of Regulatory Affairs is responsible for leading and/or participating on interdisciplinary regulatory teams responsible for defining and implementing regulatory strategy, including plans to submit Marketing Applications globally. Provides regulatory leadership on cross-functional development teams.
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The Immunology Oncology Nurse Manager is responsible for driving patient yield from enrollment to completed infusion for commercial accounts prescribing PROVENGE® (sipuleucel-T) through healthcare professional education, clinical support, and facilitation of patient navigation from apheresis cell collection through the infusion process. The role is field-based and requires close collaboration with other functions within Dendreon (e.g., Apheresis Network, Sales Teams, and Medical Affairs).
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The Director, Market Accesswill be responsible for assisting the Director of Market Access and Reimbursement in the development, implementation and management of business strategies to enhance managed care access of current and future Dendreon products through an analytical market-focused approach; providing a strategic vision and acting as a transformational agent of change for Managed Care/Payor and GPO sales strategies; managing proper allocation of resources, ROI measurement for key managed care business initiatives and improving market access, while driving incremental profit for Dendreon’s lead product PROVENGE. The assigned territory is major US plans and GPOs with visits as needed.
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Dendreon is seeking a Director for Medical Affairs Communications and Intelligence (MACI) to provide strategic and operational direction for the development and execution of field and medical affairs communications and competitive intelligence in support of the clinical immunotherapy and HEOR initiatives with Dendreon Pharmaceuticals, LLC.
The successful candidate will lead the Medical Affairs Communications and Intelligence function, and develop and execute the strategies relevant to medical communications for sipuleucel-T. These activities will include, but are not limited to, the development of scientific and medical communication resources such as slide decks, clinical/scientific FAQs, literature surveillance, and competitive intelligence collections. The role will have a key part in the organization and scientific content development for Dendreon at major scientific congresses, medical meetings, and advisory boards. The Director for MACI works closely with Corporate Communications and Training department as well as other cross-functional partners, including Medical Information, PV, Publications, HEOR, V.P. of Medical Affairs, and Clinical Development to inform and execute the medical communication strategies. The position will require a strong understanding and interpretation of the clinical, economic, and humanistic data collected and generated to support sipuleucel-T and future development compounds.
The successful candidate should have excellent communication and presentation skills, and a record of accomplishment working in a cross-functional collaborative environment. He or she should have a background in the life sciences industry with experience in translating clinical data into clear, concise evidence and communication plans for both payer and clinical audiences in both academia and community practice.
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The Accounts Payable Specialist will maintain current accounts and assist in invoicing functions, analyze expense reports to assign payments to proper cost centers, work with vendors to resolve past due invoices and reconcile monthly statements with vendors. This position reports to the Manager, Accounts Payable.
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The Quality Specialist II, Quality Manufacturing Performs a wide variety of QA activities to ensure compliance with applicable regulatory requirements.
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The Manufacturing Operations Associate is responsible for Aseptic manufacturing and assembly of clinical and commercial human blood derived components in a clean-room environment (Class 10,000/ISO7, and Class 100,000/ISO8) General responsibilities are: aseptic manufacturing and assembly of clinical and commercial human blood derived components in a clean-room environment (Class 10,000/ISO7, and Class 100,000/ISO8). This job is performed in a lab, office, or utility (noisy) environment, and this person may be required to work alternate shifts.
Ideal candidate is available to work: Monday, Tuesday, Friday: 6:30PM - 6:30AM.
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Dendreon is seeking a Medical Director, Medical Affairs to provide strategic medical affairs leadership in developing and executing medical affairs plan, overseeing medical research including clinical trials, and advancing scientific understandings of Dendreon products.
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Dendreon is seeking a dedicated Medical Science Liaison to join its Medical Affairs team. This person will have the opportunity to work with the only approved immune-oncology therapy for prostate cancer. Successful candidates will master clinical information on sipuleucel-T and speak to the immunologic basis for its therapeutic effect. This individual will serve as a resource to healthcare professionals caring for prostate cancer patients, facilitate the successful implementation of clinical trials, and provide field perspective to Dendreon.
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The Director, IT Infrastructure is responsible for acquiring, managing, and developing Dendreon’s enterprise infrastructure technology, supporting applications, service desk, policies and procedures, and governance as it relates to the company’s technology infrastructure environment. The role manages the Infrastructure team and outsourced managed service providers responsible for the service desk, systems, network, including WAN/LAN and Internet connectivity, remote access, security, storage, virtualization, cloud services, data center, voice, mobility, disaster recovery and business continuity. The position is responsible for providing oversight, implementing appropriate controls and performing regular and effective reviews of all technical aspects, including operational support activities.
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The Manager, Bioassay is responsible for the oversight, planning, coordination, and supervision of technical and operational activities in the Bioassay laboratory.
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The Sr. Quality Specialist, Computer Systems Validation individual is responsible for providing Quality & Compliance oversight to ensure compliance with Computer System Validation (CSV), Systems Development Lifecycle (SDLC) and Data Integrity.
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The Quality Control Supervisor - Bioassay is responsible for the providing daily supervision of lab operations (people, process, product) for one or more functional areas within Quality Control. Ensures the site, process, product, and personnel are compliant with regulatory requirements.
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Dendreon’s Immunotherapy Sales Specialist is responsible for achieving sales objectives in an assigned territory through the development, maintenance, and enhancement of the business. Customers include oncologists, urologists, nurses, pharmacists, pharmacy and therapeutics groups, tumor boards, teaching institutions, hospitals and formulary committees. The role is responsible for ensuring customer’s clinical conviction in the product as well as guiding the customer through the logistics process and seeing the sale through to its conclusion.
Ideal candidate locale is San Antonio or Austin, TX.
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The Director, Marketing will lead the execution of a national marketing strategy to achieve business objectives and play a cohesive role within the Commercial organization. Responsible for marketing leadership to support Provenge and build Dendreon’s brand equity. This role serves as champion of the Provenge brand and ensures it is consistently and meaningfully represented in all customer touch points. The Director, Marketing will report to the VP, Commercial Sales and Customer Relations.
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The Quality Program Manager, Sterility Assurance is responsible for planning, coordinating and facilitating microbial control activities required for Dendreon’s drug products. The role will interact with all site and cross site functions that could impact Dendreon's microbial control program including Facilities, QC Microbiology, Manufacturing, Process Sciences.
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The Supervisor of Quality is responsibile for supervising and managing the performance of a wide variety of QA activities to ensure compliance with applicable regulatory requirements
- Provides daily supervision of QA staff and activities
- Provides support in the development, implementation and maintenance of quality assurance systems
- May be responsible for one or more of the following:
- QA review and approval on GXP controlled documents
- GMP material review and disposition
- Deviation and CAPA program management
- Internal and external GXP audit program
- GMP training program
- Represents QA in cross-functional teams and projects
- Selects, develops, and evaluates personnel to ensure functional objectives are met.
